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TTCTTCACACTTGCCCTAGCTGATC[A/C]TGAGCCACAAGCAGGAAGGGCTAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 164176 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
POU2F2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
POU2F2 - POU class 2 homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001207025.2 | Intron | NP_001193954.1 | ||||
NM_001207026.1 | Intron | NP_001193955.1 | ||||
NM_001247994.1 | Intron | NP_001234923.1 | ||||
NM_002698.4 | Intron | NP_002689.1 | ||||
XM_005259010.3 | Intron | XP_005259067.1 | ||||
XM_011527040.2 | Intron | XP_011525342.1 | ||||
XM_011527041.2 | Intron | XP_011525343.1 | ||||
XM_011527042.2 | Intron | XP_011525344.1 | ||||
XM_011527043.2 | Intron | XP_011525345.2 | ||||
XM_017026884.1 | Intron | XP_016882373.1 | ||||
XM_017026885.1 | Intron | XP_016882374.1 | ||||
XM_017026886.1 | Intron | XP_016882375.1 | ||||
XM_017026887.1 | Intron | XP_016882376.1 | ||||
XM_017026888.1 | Intron | XP_016882377.1 | ||||
XM_017026889.1 | Intron | XP_016882378.1 | ||||
XM_017026890.1 | Intron | XP_016882379.1 | ||||
XM_017026891.1 | Intron | XP_016882380.1 | ||||
XM_017026892.1 | Intron | XP_016882381.1 | ||||
XM_017026893.1 | Intron | XP_016882382.1 | ||||
XM_017026894.1 | Intron | XP_016882383.1 | ||||
XM_017026895.1 | Intron | XP_016882384.1 | ||||
XM_017026896.1 | Intron | XP_016882385.1 |